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Data / Medical devices / Stimulator, Invasive Bone Growth

Stimulator, Invasive Bone Growth (LOE): 4 FDA-registered makers in 1 country

4 establishments in 1 country are registered with the FDA to make Stimulator, Invasive Bone Growth (product code LOE, Class 3). 3 of them have a 510(k) clearance or PMA approval on file and 1 has a recall event. The FDA has issued 0 510(k) clearances under this code, and lists 2 recall events (2 Class I). FDA data exported November 2, 2026.

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Product code
LOE
Device class
3
Medical specialty
Unknown

Makers by country

CountryMakers
United States4

Makers of Stimulator, Invasive Bone Growth

Registered establishments that manufacture, contract manufacture, remanufacture, reprocess or own the specification of this device, with the 510(k) clearances, PMA approvals and recalls the FDA files under each. Best documented first.

MakerLocationRole510(k) clearancesLatest clearancePMA approvalsRecall eventsClass ISource
Ebi Patient Care, Inc.Guaynabo, PR, United StatesManufacturer0211api.fda.gov
Ebi, LLCParsippany, NJ, United StatesComplaint file establishment, Specification developer0200api.fda.gov
Highridge Medical, LLCWestminster, CO, United StatesSpecification developer0200api.fda.gov
Olive Branch Distribution CenterOlive Branch, MS, United StatesContract manufacturer0000api.fda.gov

Updated November 2, 2026. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.